Journal Information
Vol. 101. Issue 7.
Pages 637-640 (September 2010)
Share
Share
Download PDF
More article options
Vol. 101. Issue 7.
Pages 637-640 (September 2010)
Case report
Full text access
New Mutation in the Birt Hogg Dube Gene
Nueva mutación en el síndrome de Birt Hogg Dubé
Visits
5303
L. Sempaua,
Corresponding author
leticiasempau@gmail.com

Corresponding author.
, I. Ruiza, A. González-Moránb, X. Susannac, T.V.O. Hansend
a Servicio de Dermatología, Complejo Asistencial de León, León, Spain
b Servicio de Anatomía Patológica, Complejo Asistencial de León, León, Spain
c Director Técnico de Balagué Center, Barcelona, Spain
d Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark
This item has received
Article information
Abstract

Patients with Birt-Hogg-Dube syndrome have an increased risk of developing hamartomas of the pilosebaceous unit, renal tumors of various types, lung cysts, and spontaneous pneumothorax. We present the case of a 54-year-old woman with a long history of whitish papules in the central region of the face and a family history of similar lesions. Biopsy and genetic study revealed a new mutation of the gene involved in Birt-Hogg-Dube syndrome.

Keywords:
Fibrofolliculoma
Acrochordon
Birt-Hogg-Dube syndrome
Mutation
Resumen

El Birt Hogg Dubé es un síndrome que predispone a la aparición de hamartomas del folículo pilosebáceo y a mayor riesgo de presentar tumores renales de diversa estirpe, quistes pulmonares y neumotórax espontáneos.

Presentamos el caso de una mujer de 54 años que presenta desde hace años pápulas blanquecinas centrofaciales e historia familiar de esas mismas pápulas. Tras biopsia y estudio genético de la paciente se detecta una nueva mutación en el gen implicado en este síndrome.

Palabras clave:
Fibrofoliculoma
Acrocordón
Síndrome Birt Hogg Dubé
Mutación
Full text is only aviable in PDF
References
[1.]
S.K. Khoo, S. Giraud, K. Kahnoski, J. Chen, O. Motorna, R. Nickolov, et al.
Clinical and genetic studies of Birt-Hogg-Dube syndrome.
J Med Genet, 39 (2002), pp. 906-912
[2.]
M.L. Nickerson, M.B. Warren, J.R. Toro, V. Matrosova, G. Glenn, M.L. Turner, et al.
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome.
Cancer Cell, 2 (2002), pp. 157-164
[3.]
C. De la Torre, C. Ocampo, I.G. Doval, A. Losada, M.J. Cruces.
Acrochordons are not a component of the Birt-Hogg-Dubé syndrome - does this syndrome exist? Case reports and review of the literature.
Am J Dermatol, 21 (1999), pp. 369-374
[4.]
J. Toro, P.H. Duray, G.M. Glenn, T. Darling, B. Zbar, W.M. Linehan, et al.
Birt-Hogg-Dube syndrome: a novel marker of kidney neoplasia.
Arch Dermatol, 135 (1999), pp. 1195-1202
[5.]
B. Zbar, G. Alvord, G. Glenn, M. Turner, C.P. Pavlovich, L.S. Schmidt, et al.
Risk of renal and colon neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome.
Cancer Epidemiol Biomarkers Prev, 11 (2002), pp. 393-400
[6.]
O. Binet, J. Robin, M. Vicart, G. Ventura, E. Beltzer-Garelly.
Fibromes périfolliculaires, polypose colique familiale, pneumothorax spontanés familiaux.
Ann Dermatol Venereol, 113 (1986), pp. 928-930
[7.]
T. Schulz, W. Hartschuh.
Birt-Hogg-Dubé syndrome and Hornstein-Knickenberg syndrome are the same. Different sectioning technique as the cause of different histology.
J Cutan Pathol, 26 (1999), pp. 55-61
[8.]
L.S. Schmidt, M.B. Warren, M.L. Nickerson, G. Weirich, V. Matrosova, J.R. Toro, et al.
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.
Am J Hum Genet, 69 (2001), pp. 876-882
[9.]
M.B. Warren, C.A. Torres-Cabala, M.L. Turner, M.J. Merino, V.Y. Matrosova, M.L. Nickerson, et al.
Expression of Birt-Hogg-Dubé gene mRNA in normal and neoplastic human tissues.
Mod Pathol, 17 (2004), pp. 998-1011
[10.]
M. Baba, S.B. Hong, N. Sharma, M.B. Warren, M.L. Nickerson, A. Iwamatsu, et al.
Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signalling.
Proc Natl Acad Sci USA, 103 (2006), pp. 15552-15557
[11.]
J.R. Toro, M.H. Wei, G.M. Glenn, M. Weinreich, O. Toure, C. Vocke, et al.
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dube’ syndrome: a new series of 50 families and a review of published reports.
J Med Genet, 45 (2008), pp. 321-331
[12.]
F.H. Menko, M.A. van Steensel, S. Giraud, L. Friis-Hansen, S. Richard, S. Ungari, M. Nordenskjöld, T.V. Hansen, J. Solly, E.R. Maher, et al.
European BHD Consortium. Birt-Hogg-Dubé syndrome: diagnosis and management.
Lancet Oncol, 10 (2009), pp. 1199-1206
[13.]
Welsch, A. Krunic, M.M. Medenica.
Birt-Hogg-Dubé Syndrome.
Int J Dermatol, 44 (2005), pp. 668-673
[14.]
N.M. Lindor, J. Hand, P.A. Burch, L.E. Gibson.
Birt-Hogg-Dube Syndrome: an autosomal dominant disorder with predisposition to cancers of the kidney, fibrofolliculomas, and focal cutaneous mucinosis.
Int J Dermatol, 40 (2001), pp. 653-656
Copyright © 2010. Academia Española de Dermatología y Venereología and Elsevier España, S.L.
Idiomas
Actas Dermo-Sifiliográficas
Article options
Tools
es en

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?